The GENDULF algorithm: mining transcriptomics to uncover modifier genes for monogenic diseases

Modifier genes are believed to account for the clinical variability observed in many Mendelian disorders, but their identification remains challenging due to the limited availability of genomics data from large patient cohorts. Here, we present GENDULF (GENetic moDULators identiFication), one of the...

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Detalhes bibliográficos
Publicado no:Mol Syst Biol
Main Authors: Auslander, Noam, Ramos, Daniel M, Zelaya, Ivette, Karathia, Hiren, Crawford, Thomas O., Schäffer, Alejandro A, Sumner, Charlotte J, Ruppin, Eytan
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Methods
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7754056/
https://ncbi.nlm.nih.gov/pubmed/33438800
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/msb.20209701
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